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Journal Abstract Search
115 related items for PubMed ID: 2526881
1. Cystathioninuria in Down's syndrome. Hestnes A, Borud O, Lunde H, Gjessing L. J Ment Defic Res; 1989 Jun; 33 ( Pt 3)():261-5. PubMed ID: 2526881 [Abstract] [Full Text] [Related]
2. [Congenital cystathioninuria. B6-dependent]. Bravo Mata M, Escribano Rey MD, Alonso Martín A, Alonso Fernández JR. An Esp Pediatr; 1993 Sep; 39(3):260-4. PubMed ID: 8250445 [No Abstract] [Full Text] [Related]
3. Primary cystathioninuria. Methionine load tests and response to pyridoxine. Bremer HJ, Endres W. Helv Paediatr Acta; 1972 Nov; 27(5):525-36. PubMed ID: 4640904 [No Abstract] [Full Text] [Related]
5. Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria. Bittles AH, Carson NA. J Med Genet; 1974 Jun; 11(2):121-2. PubMed ID: 4841081 [No Abstract] [Full Text] [Related]
6. Distribution of sulfur in urine of patients with cystathioninuria before and during administration of pyridoxine. Frimpter GW, Kozlowski KK, Horwith M. Metabolism; 1976 Mar; 25(3):355-60. PubMed ID: 1250167 [Abstract] [Full Text] [Related]
8. Cystathioninuria and homocystinuria. Levy HL, Mudd SH, Uhlendorf BW, Madigan PM. Clin Chim Acta; 1975 Jan 06; 58(1):51-9. PubMed ID: 1122632 [Abstract] [Full Text] [Related]
9. Cystathioninuria, renal iminoglycinuria and...alpha 1-antitrypsin...deficiency in the same family: relevance in medical practice. Halal F, Scriver CR, Cox DW, Jaber L, Varsano I. Can Med Assoc J; 1979 Jul 07; 121(1):64-8. PubMed ID: 313837 [No Abstract] [Full Text] [Related]
10. Quantitative analysis of cystathionine and perhydro-1,4-thiazepine-3,5-dicarboxylic acid in the urine of a patient with cystathioninuria using isotachophoresis. Kodama H, Sasaki K, Mikasa H, Cavallini D, Ricci G. J Chromatogr; 1984 Nov 09; 311(1):183-8. PubMed ID: 6520162 [No Abstract] [Full Text] [Related]
11. Identification of N-acetyl-S-(3-oxo-3-carboxy-n-propyl)cysteine in the urine of a patient with cystathioninuria using LC/APCI-MS. Zhang J, Masuoka N, Ubuka T, Sugahara K, Kodama H. J Inherit Metab Dis; 1995 Nov 09; 18(6):675-81. PubMed ID: 8750604 [Abstract] [Full Text] [Related]
14. Cystathionase deficiency: evidence for genetic heterogeneity in primary cystathioninuria. Pascal TA, Gaull GE, Beratis NG, Gillam BM, Tallan HH. Pediatr Res; 1978 Feb 09; 12(2):125-33. PubMed ID: 417288 [No Abstract] [Full Text] [Related]
15. Cystathioninuria in a profoundly mentally retarded woman with spastic tetraplegia, deafness and abnormal liver function tests. Hestnes A, Borud O, Lunde H, Gjessing LR. J Ment Defic Res; 1987 Sep 09; 31 ( Pt 3)():299-301. PubMed ID: 3681958 [Abstract] [Full Text] [Related]
16. Identification of NAc-HCPC and NAc-beta-CEC, and qualitative analyses of sulphur amino acids in the urine of a patient with cystathioninuria using liquid chromatography/atmospheric pressure ionization mass spectrometry. Watanabe H, Fujita Y, Sugahara K, Kodama H, Ohmori S. Biol Mass Spectrom; 1991 Oct 09; 20(10):602-8. PubMed ID: 1793738 [Abstract] [Full Text] [Related]
17. Identification of new cystathionine mono-oxo acids, S-(3-oxo-3-carboxy-n-propyl) cysteine and S-(2-oxo-2-carboxyethyl) homocysteine, in the urine of a patient with cystathioninuria. Okada T, Takechi T, Wakiguchi H, Kurashige T, Sugahara K, Kodama H. Arch Biochem Biophys; 1993 Sep 09; 305(2):385-91. PubMed ID: 8373176 [Abstract] [Full Text] [Related]
18. [Seesaw nystagmus: symptom of a biochemical disorder (author's transl)]. Rych K. Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1977 Feb 23; 201(3):221-8. PubMed ID: 300573 [Abstract] [Full Text] [Related]
19. [Secondary cystathioninuria due to vitamin B 6 deficiency in familial neuroblastoma]. Plöchl E. Padiatr Padol; 1976 Feb 23; 11(2-2):444-68. PubMed ID: 967508 [Abstract] [Full Text] [Related]
20. Renal impairment in urate excretion in patients with Down's syndrome. Nishida Y, Akaoka I, Kobayashi M, Maruki K, Oshima Y. J Rheumatol; 1979 Feb 23; 6(1):103-7. PubMed ID: 155745 [Abstract] [Full Text] [Related] Page: [Next] [New Search]